Endothelial Connexin37 and Connexin40 participate in basal but not agonist-induced NO release.
Détails
Télécharger: 26198171_BIB_C0DFD70CCF17.pdf (1705.10 [Ko])
Etat: Public
Version: Final published version
Etat: Public
Version: Final published version
ID Serval
serval:BIB_C0DFD70CCF17
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Endothelial Connexin37 and Connexin40 participate in basal but not agonist-induced NO release.
Périodique
Cell Communication and Signaling : Ccs
ISSN
1478-811X (Electronic)
ISSN-L
1478-811X
Statut éditorial
Publié
Date de publication
2015
Peer-reviewed
Oui
Volume
13
Pages
34
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: epublish
Publication Status: epublish
Résumé
BACKGROUND: Connexin37 (Cx37) and Cx40 are crucial for endothelial cell-cell communication and homeostasis. Both connexins interact with endothelial nitric oxide synthase (eNOS). The exact contribution of these interactions to the regulation of vascular tone is unknown.
RESULTS: Cx37 and Cx40 were expressed in close proximity to eNOS at cell-cell interfaces of mouse aortic endothelial cells. Absence of Cx37 did not affect expression of Cx40 and a 50 % reduction of Cx40 in Cx40(+/-) aortas did not affect the expression of Cx37. However, absence of Cx40 was associated with reduced expression of Cx37. Basal NO release and the sensitivity for ACh were decreased in Cx37(-/-) and Cx40(-/-) aortas but not in Cx40(+/-) aortas. Moreover, ACh-induced release of constricting cyclooxygenase products was present in WT, Cx40(-/-) and Cx40(+/-) aortas but not in Cx37(-/-) aortas. Finally, agonist-induced NO-dependent relaxations and the sensitivity for exogenous NO were not affected by genotype.
CONCLUSIONS: Cx37 is more markedly involved in basal NO release, release of cyclooxygenase products and the regulation of the sensitivity for ACh as compared to Cx40.
RESULTS: Cx37 and Cx40 were expressed in close proximity to eNOS at cell-cell interfaces of mouse aortic endothelial cells. Absence of Cx37 did not affect expression of Cx40 and a 50 % reduction of Cx40 in Cx40(+/-) aortas did not affect the expression of Cx37. However, absence of Cx40 was associated with reduced expression of Cx37. Basal NO release and the sensitivity for ACh were decreased in Cx37(-/-) and Cx40(-/-) aortas but not in Cx40(+/-) aortas. Moreover, ACh-induced release of constricting cyclooxygenase products was present in WT, Cx40(-/-) and Cx40(+/-) aortas but not in Cx37(-/-) aortas. Finally, agonist-induced NO-dependent relaxations and the sensitivity for exogenous NO were not affected by genotype.
CONCLUSIONS: Cx37 is more markedly involved in basal NO release, release of cyclooxygenase products and the regulation of the sensitivity for ACh as compared to Cx40.
Mots-clé
Acetylcholine/metabolism, Animals, Aorta/cytology, Aorta/physiology, Connexins/genetics, Connexins/metabolism, Endothelium, Vascular/cytology, Endothelium, Vascular/physiology, Gene Deletion, Gene Expression Regulation, Genotype, Mice, Mice, Inbred C57BL, Nitric Oxide/agonists, Nitric Oxide/metabolism, Nitric Oxide Synthase Type III/metabolism, Vasoconstriction, Vasodilation
Pubmed
Web of science
Open Access
Oui
Création de la notice
24/08/2015 16:38
Dernière modification de la notice
20/08/2019 15:35